Role of homocysteine & MTHFR C677T gene polymorphism as risk factors for coronary artery disease in young Indians

BACKGROUND & OBJECTIVES: Hyperhomocysteinaemia (HCA) either due to mutation of MTHFR gene or deficiency of vitamin B(12) and folic acid, has been reported as a risk factor for coronary artery disease (CAD). The present study was aimed to determine plasma homocysteine (Hcy) levels and to evaluate...

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Detalles Bibliográficos
Autores principales: Gupta, Santosh Kumar, Kotwal, Jyoti, Kotwal, Atul, Dhall, Anil, Garg, Salil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385234/
https://www.ncbi.nlm.nih.gov/pubmed/22664498

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385234/
https://www.ncbi.nlm.nih.gov/pubmed/22664498

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